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J Dermatol ; 39(5): 466-9, 2012 May.
Article in English | MEDLINE | ID: mdl-22011194

ABSTRACT

Although disseminated nocardiosis has been increasing with the expansion of immunosuppressive therapy and improvement in diagnostic methods, muscle abscess is a rare complication. There have been only nine case reports of muscle abscess due to Nocardia infection in the English-language published work. We present a case of muscle abscess with disseminated nocardiosis, and review the published work. The patient had been taking prednisolone at 20 mg a day for autoimmune hemolytic anemia for 14 years. She presented with erythema on her thigh resembling cellulitis. Computed tomography showed muscle abscess. The isolated organism was identified as Nocardia farcinica employing polymerase chain reaction and antibiotic sensitivity testing. The diagnosis of muscle abscess due to nocardiosis can be easily missed because there are no characteristic symptoms.


Subject(s)
Abscess/etiology , Anemia, Hemolytic, Autoimmune/complications , Muscular Diseases/etiology , Nocardia Infections/complications , Abscess/drug therapy , Anemia, Hemolytic, Autoimmune/drug therapy , Anti-Bacterial Agents/therapeutic use , Brain Abscess/drug therapy , Brain Abscess/etiology , Female , Humans , Immunosuppressive Agents/adverse effects , Middle Aged , Muscular Diseases/drug therapy , Nocardia/isolation & purification , Nocardia Infections/drug therapy , Nocardia Infections/etiology , Prednisolone/adverse effects , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
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